Canonical Allele Identifier: CA507701091

Gene: CIC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42272377C>T , CM000681.2:g.42272377C>T	GRCh38
NC_000019.9:g.42776529C>T , CM000681.1:g.42776529C>T	GRCh37
NC_000019.8:g.47468369C>T	NCBI36
NG_042060.1:g.8841C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001386298.1:c.594C>T MANE Select	NP_001373227.1:p.Asp198=
ENST00000681038.1:c.594C>T MANE Select	ENSP00000505728.1:p.Asp198=
NM_001304815.1:c.594C>T	NP_001291744.1:p.Asp198=
NM_001304815.2:c.594C>T	NP_001291744.1:p.Asp198=
NM_001379480.1:c.594C>T	NP_001366409.1:p.Asp198=
NM_001379482.1:c.594C>T	NP_001366411.1:p.Asp198=
ENST00000572681.6:c.594C>T	ENSP00000459719.1:p.Asp198=
XM_011526660.1:c.594C>T	XP_011524962.1:p.Asp198=
XM_011526660.2:c.594C>T	XP_011524962.1:p.Asp198=
XM_011526661.1:c.594C>T	XP_011524963.1:p.Asp198=
XM_011526661.2:c.594C>T	XP_011524963.1:p.Asp198=
XM_011526662.1:c.594C>T	XP_011524964.1:p.Asp198=
XM_011526662.2:c.594C>T	XP_011524964.1:p.Asp198=
XM_011526663.1:c.594C>T	XP_011524965.1:p.Asp198=
XM_011526663.2:c.594C>T	XP_011524965.1:p.Asp198=
XM_011526664.1:c.594C>T	XP_011524966.1:p.Asp198=
XM_011526664.2:c.594C>T	XP_011524966.1:p.Asp198=
XM_011526665.1:c.594C>T	XP_011524967.1:p.Asp198=
XM_011526665.2:c.594C>T	XP_011524967.1:p.Asp198=
XM_011526666.1:c.594C>T	XP_011524968.1:p.Asp198=
XM_011526666.2:c.594C>T	XP_011524968.1:p.Asp198=
XM_011526667.1:c.594C>T	XP_011524969.1:p.Asp198=
XM_011526667.2:c.594C>T	XP_011524969.1:p.Asp198=
XM_024451432.1:c.594C>T	XP_024307200.1:p.Asp198=
XM_024451433.1:c.594C>T	XP_024307201.1:p.Asp198=
XR_002958286.1:n.704C>T
XR_002958287.1:n.704C>T
XR_002958288.1:n.704C>T
XR_002958289.1:n.704C>T
XR_002958290.1:n.704C>T
XR_935775.1:n.705C>T
XR_935776.1:n.705C>T
XR_935777.1:n.705C>T
XR_935778.1:n.705C>T
XR_935778.2:n.704C>T
XR_935779.1:n.705C>T
XR_935779.2:n.704C>T